Structure Database (LMSD)
Common Name
Aplysterol
Systematic Name
(25S)-24R,26-dimethylcholest-5-en-3β-ol
Synonyms
- (25S)-26-methylcampest-5-en-3beta-ol
No other lipid differing only in stereochemistry/bond geometry found
3D model of Aplysterol
Please note: Where there are chiral atoms but the stereochemistry is undefined, the 3D model takes an arbitrary conformation
Classification
Category
Main Class
Sub Class
References
Taxonomy Information
Curated from
NCBI taxonomy class
Reference
Aplysina aerophoba
(#289389)
Demospongiae
(#6042)
Marine sterols with a new pattern of side-chain alkylation from the sponge Aplysina(=Verongia)Aerophoba,
J. Chem. Soc., Perkin Trans. 1,, 1972
J. Chem. Soc., Perkin Trans. 1,, 1972
DOI:
10.1039/P19720002132
String Representations
InChiKey (Click to copy)
KBCUEZZDVQYXRC-VMQVIPOFSA-N
InChi (Click to copy)
InChI=1S/C29H50O/c1-7-19(2)20(3)8-9-21(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h10,19-21,23-27,30H,7-9,11-18H2,1-6H3/t19-,20+,21+,23-,24-,25+,26-,27-,28-,29+/m0/s1
SMILES (Click to copy)
[C@]12(CC=C3C[C@@H](O)CC[C@]3(C)[C@@]1([H])CC[C@]1(C)[C@@]([H])([C@@](C)([H])CC[C@@H](C)[C@]([H])(CC)C)CC[C@@]21[H])[H]
Other Databases
Calculated Physicochemical Properties
Heavy Atoms
30
Rings
4
Aromatic Rings
0
Rotatable Bonds
6
Van der Waals Molecular Volume
466.97
Topological Polar Surface Area
20.23
Hydrogen Bond Donors
1
Hydrogen Bond Acceptors
1
logP
8.31
Molar Refractivity
128.73
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Updated at
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